A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162931



Internal ID21499634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86611736..86611736hg38UCSC Ensembl
chr9:89226651..89226651hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633233
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162931
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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